Recruiting
Phase 2

Vedolizumab

Sponsor:

Ottawa Hospital Research Institute

Code:

NCT03147859

Conditions

HIV-infection/AIDS

Eligibility Criteria

Sex: All

Age: 18 - 65

Healthy Volunteers: Not accepted

Interventions

Vedolizumab (brand name Entyvio)

Study Details

Brief summary:

Background:

In nearly all people with human immunodeficiency virus (HIV) infection, immunity cannot either control or eradicate the infection. There are good medicinal treatments, collectively called "ART" (antiretroviral therapy) which control HIV infection by suppressing the virus in the bloodstream. ART is needed for life, and if a person stops taking ART the HIV infection returns in the bloodstream. So, there is good treatment, but no cure. The researchers want to test whether a period of treatment with vedolizumab can be used to control HIV infection in the bloodstream in persons with HIV on ART, after stopping ART.

Objective:

To determine whether vedolizumab is safe and tolerable in people with HIV, to assess the safety of an analytical treatment interruption (ATI), and to determine whether vedolizumab can control HIV infection in the bloodstream without the use of ART.

Eligibility:

Adults 18-65 with HIV who are being treated with ART

Design:

Participants will be screened with: Physical exam, medical history, blood and urine tests Participants will have a baseline visit which will include repeat of the screening testing.

Participants will then present for their first study visit which will include: receiving vedolizumab infusions through an arm vein, repeats of the baseline testing. Participants will then have serial visits on a pre-specific schedule to receive ongoing vedolizumab doses every 2-4 weeks until week 20. Each visit will also include repeat of the baseline tests.

After week 6 and before week 7 patients will discontinue ART. After the final infusion of vedolizumab at week 20 patients will continue to be assessed with physical exam, medical history, and repeat of the baseline testing every 4 weeks up to 1 year.

ART will be re-started for participants if the level of HIV in the blood becomes too high, persists for too long, or if the CD4 count decreases by too much.

Conditions

HIV-infection/AIDS

Study ID

NCT03147859

Start date

Nov 1, 2017

Status verified date

May, 2023

Completion date

Dec 31, 2023

Anticipated

Primary completion date

Dec 31, 2023

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 65

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Adult (≥ 18 to 65 years) with HIV infection.
2. Nadir CD4 T cell count ≥ 200 and current CD4 T cell count > 500 cells/mcL
3. Adherent on ART 2 to 9 years with sustained pVL ≤ 50 copies/mL
4. Ability to comprehend and provided informed consent

Exclusion Criteria:

1. Past AIDS-defining or AIDS-related immune deficiency diseases
2. Past drug-resistant HIV or ART-refractory pVL response
3. Current hepatitis B or C virus infection, or untreated latent TB infection
4. Clinically significant concurrent health condition.
5. Pregnancy, lactation, or non-adherence with contraception if fertile.

Study Design

Enrollment

10 participants

Anticipated

Allocation

Non randomized

Intervention Model

Sequential

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Group A-150mg dose of vedolizumab per infusion followed by ATI - Low Dose

\* Please note that the previous low dose arm was 75mg of vedolizumab per infusion, but no participant was ever given this dose. The study will have a 20-week treatment phase and a 28-week follow-up phase over one year. Intravenous infusion of 150 mg of vedolizumab per infusion per visit schedule will be administered to 4 participants. The visit schedule will be the same for each group - Infusion at weeks 0, 2, 5, 8 and every 4 weeks thereafter up to 40 weeks for at least 7 doses as tolerated. ATI will begin between weeks 6 and 7, and infusions continued at weeks 8, 12, 16 and 20.

experimental: Group B-300mg dose of vedolizumab per infusion followed by ATI - Mid Dose

The study will have a 20-week treatment phase and a 28-week follow-up phase over one year. Intravenous infusion of 300 mg of vedolizumab per infusion per visit schedule will be administered to 4 participants. The visit schedule will be the same for each group - Infusion at weeks 0, 2, 5, 8 and every 4 weeks thereafter up to 40 weeks for at least 7 (and up to 12) doses as tolerated. ATI will begin between week 10, and infusions continued at weeks 12, 16 and 20. Infusions may also be given at weeks 24, 28, 32, 36 and 40 depending on tolerance and pVL response.

experimental: Group C-600mg dose of vedolizumab per infusion followed by ATI - High Dose

The study will have a 20-week treatment phase and a 28-week follow-up phase over one year. Intravenous infusion of 600 mg of vedolizumab per infusion per visit schedule will be administered to 4 participants. The visit schedule will be the same for each group - Infusion at weeks 0, 2, 5, 8 and every 4 weeks thereafter up to 40 weeks for at least 7 (and up to 12) doses as tolerated. ATI will begin between week 10, and infusions continued at weeks 12, 16 and 20. Infusions may also be given at weeks 24, 28, 32, 36 and 40 depending on tolerance and pVL response.

Interventions

Vedolizumab (brand name Entyvio)

IV infusion

Primary outcome measure

  • Vedolizumab safety and tolerance [ Time Frame: 6 months vedolizumab treatments, serial assessments over 12 months ]

Central Contacts and Locations

Central contacts

Michaeline McGuinty, MD

289-668-3798mimcguinty@toh.ca

Locations

The Ottawa Hospital -General Campus

Recruiting

Ottawa, Ontario, Canada, K1H 8L6

Contacts

Donald W Cameron, MD

613-737-8923bcameron@ohri.ca

Principal Investigator:

Donald W Cameron, MD

More Information

Sponsor

Ottawa Hospital Research Institute

Last update posted

May 11, 2023

Last verified

May, 2023

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Ottawa Hospital Research Institute on 2023-05-11.